Evidence map›Paper›PMID 32292393›Full record

ArticleFrontiers in microbiology2020

Identifying Metabolic Inhibitors to Reduce Bacterial Persistence.

Sayed Golam Mohiuddin, Thuy Hoang, Adesola Saba, Prashant Karki, Mehmet A Orman

Open access · goldAbstract read
In one paragraph

Article in Frontiers in microbiology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
5.0field-weighted citation impact, top 4% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

20 citing papers in PubMed, 44 citations in OpenAlex.

  1. Article
  2. Article
  3. UNRAVELING CRP/cAMP-MEDIATED METABOLIC REGULATION INbioRxiv : the preprint server for biology · 2025
    Article
  4. Article
  5. Article
  6. Article
  7. Microbiology spectrum · 2023
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. mBio · 2022
    Article
  15. Single-cell Raman spectroscopy identifiesFrontiers in microbiology · 2022
    Article
  16. Review
  17. Review
  18. Review
  19. Monitoring Persister Resuscitation with Flow Cytometry.Methods in molecular biology (Clifton, N.J.) · 2021
    Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 1 institution in 1 country.

Sayed Golam MohiuddinDepartment of Chemical and Biomolecular Engineering, University of Houston, Houston, TX, United States.
Thuy HoangDepartment of Chemical and Biomolecular Engineering, University of Houston, Houston, TX, United States.
Adesola SabaDepartment of Chemical and Biomolecular Engineering, University of Houston, Houston, TX, United States.
Prashant KarkiDepartment of Chemical and Biomolecular Engineering, University of Houston, Houston, TX, United States.
Mehmet A OrmanDepartment of Chemical and Biomolecular Engineering, University of Houston, Houston, TX, United States.
University of Houston · US

Funding

Investigating "viable but non-culturable" Cell and Persister Formation MechanismsK22AI125468 · NIAID · UNIVERSITY OF HOUSTON · PI ORMAN, MEHMET A. · 2018 to 2019
$270k
NIAID NIH HHS K22 AI125468
6 · The paper itself

Abstract

Bacterial persisters are rare phenotypic variants that are temporarily tolerant to high concentrations of antibiotics. We have previously discovered that stationary-phase-cell subpopulations exhibiting high redox activities were less capable of producing proteins and resuming growth upon their dilution into fresh media. The redox activities of these cells were maintained by endogenous protein and RNA degradation, resulting in self-inflicted damage that transiently repressed the cellular functions targeted by antibiotics. Here, we showed that pretreatment of stationary-phase cells with an ATP synthase inhibitor, chlorpromazine hydrochloride (CPZ), significantly reduced stationary-phase-redox activities and protein degradation, and yielded cells that were more susceptible to cell death when exposed to antibiotics in fresh media. Leveraging this knowledge, we developed an assay integrating a degradable fluorescent protein system and a small library, containing FDA-approved drugs and antibiotics, to detect medically relevant drugs that potentially target persister metabolism. We identified a subset of chemical inhibitors, including polymyxin B, poly-L-lysine and phenothiazine anti-psychotic drugs, that were able to reduce the persistence phenotype in

Indexed as

drug screeningmetabolic inhibitorspersister cellsstationary-phase metabolismviable but non-culturable cells

Identifiers

PMID32292393
PMCPMC7118205
OpenAlexW3013315776

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.